Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11907840-11908469 | Common:48; Rare:477 | ||||
chr1:11908876-11909096 | Common:2; Rare:60 | ||||
chr1:12001584-12001984 | Common:5; Rare:154; Clinvar:2; Clinvar (benign):4 | ||||
chr1:12047507-12047907 | Common:1; Rare:114 | ||||
chr1:12053831-12054351 | Common:10; Rare:214 | ||||
chr1:12175045-12175316 | Common:2; Rare:70 | ||||
chr1:12184839-12185596 | Common:13; Rare:287 | ||||
chr1:12619194-12619594 | Common:1; Rare:104 | ||||
chr1:14404900-14405450 | Common:5; Rare:120 | ||||
chr1:14597630-14597920 | Rare:40 | ||||
chr1:14627306-14627706 | Common:2; Rare:112 | ||||
chr1:14732901-14733451 | Common:6; Rare:167 | ||||
chr1:15088490-15088950 | Common:3; Rare:95 | ||||
chr1:15214536-15214844 | Common:2; Rare:66 | ||||
chr1:15384390-15384710 | Common:2; Rare:68 |